Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3804099 | 0.627 | 0.680 | 4 | 153703504 | synonymous variant | T/C | snv | 0.40 | 0.48 | 40 | |
rs3815652 | 0.925 | 0.160 | 7 | 33873792 | intron variant | C/T | snv | 0.19 | 3 | ||
rs4788172 | 0.925 | 0.120 | 16 | 29656932 | regulatory region variant | G/A | snv | 0.12 | 2 | ||
rs2072069 | 0.925 | 0.120 | 17 | 34357972 | intron variant | G/A | snv | 0.47 | 2 | ||
rs1052632 | 0.925 | 0.080 | 1 | 181051094 | non coding transcript exon variant | G/A;C | snv | 2 | |||
rs12596308 | 0.925 | 0.120 | 16 | 29679875 | intron variant | C/A;T | snv | 2 | |||
rs17842268 | 0.925 | 0.120 | 16 | 29672859 | intron variant | T/C | snv | 0.36 | 2 | ||
rs7932766 | 0.925 | 0.080 | 11 | 126292967 | synonymous variant | C/T | snv | 0.18 | 0.19 | 2 | |
rs352142 | 0.925 | 0.120 | 3 | 52232366 | intron variant | A/C | snv | 7.5E-02 | 2 | ||
rs352143 | 0.925 | 0.120 | 3 | 52230891 | synonymous variant | T/C | snv | 0.17 | 0.23 | 2 |